Engineering Manager
Tipperary
Permanent
Permanent
Engineer Manager – Clonmel
Our Client is one of the world's leading vascular care businesses. They are uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Their broad line of vascular devices–which includes vessel closure, endovascular and coronary technologies–are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
You will manage teams within the Pharmaceutical/Biological Process Sub-Function. You will focus is on policy and strategy implementation and control rather than development.
Purpose of the Job
Provides support to the manufacturing organisation to facilitate efficient operations within the production area, optimise existing processes, and ensure that production goals are met. Monitors performance of equipment, machines, and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with research and development organisations to integrate new products or processes into the existing manufacturing area.
Major Responsibilities
Our Client is one of the world's leading vascular care businesses. They are uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Their broad line of vascular devices–which includes vessel closure, endovascular and coronary technologies–are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
You will manage teams within the Pharmaceutical/Biological Process Sub-Function. You will focus is on policy and strategy implementation and control rather than development.
Purpose of the Job
Provides support to the manufacturing organisation to facilitate efficient operations within the production area, optimise existing processes, and ensure that production goals are met. Monitors performance of equipment, machines, and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with research and development organisations to integrate new products or processes into the existing manufacturing area.
Major Responsibilities
- Implements a staffing plan by identifying resource requirements, writing justifications for additional personnel, obtaining approval for changes, and coordinating the selection process with human resources.
- Develops direct reports by securing appropriate training, assigning progressively challenging tasks, applying progressive disciplinary action as appropriate and conducting formal written and verbal performance reviews.
- Monitors daily work operations and provides direction and guidance to lower-level supervisors, experienced exempt employees, or skilled nonexempt staff to achieve unit or project goals.
- Interacts with internal and external customers, by meeting regularly, responding to requests and explaining procedures. Interprets and executes policies that affect work processes and personnel within the assigned organizational unit.
- Contributes to the development of operational policies and procedures that affect personnel within the assigned organizational unit. Monitors compliance with company policies and procedures for example compliance with Food and Drug Administration (FDA), British Standards Institution (BSI), relevant employment law etcetera (etc.).
- Monitors internal and external indicators by reviewing reports and newsletters, reading organizational literature, meeting with peers and reading departmental reports. Contributes to the development and monitoring of area budget through regular analysis of cost and spending.
- Participates in validation activity. Role may vary between providing input to owning activities such as protocol/report writing and managing execution of validation activities.
- National Framework of Qualifications (NFQ) level 7 qualification in a relevant discipline and 6+ years of related work experience or an equivalent combination of education and work experience.
- Experience in monitoring progress of exempt individuals, teams, supervisors, or nonexempt technical individuals toward departmental goals.
- Proven experience monitoring costs of projects and of human and material resources within a department or unit.
